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Selective ligation of thoracic duct to prevent postoperative thylothorax using near-infrared thoracoscope in surgeries for lung cancer

Selective ligation of thoracic duct to prevent postoperative thylothorax using near-infrared thoracoscope in surgeries for lung cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076867
Enrollment
Unknown
Registered
2023-10-23
Start date
2023-10-23
Completion date
Unknown
Last updated
2023-10-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

lung cancer

Interventions

treatment group:slective ligation of thoracic duct using near-infrared thoracoscope
control group (conventional operation):NA

Sponsors

Department of Thoracic Surgery, Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients are older than 18 years, and younger than 80 years; 2. Patients performing right lung resection and systematic lymphadenectomy; 3. Patients with the pathological diagnosis of lung cancer; 4. Patients who signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of pleuritis; 2. Patients with a history of injury or surgery of thoracic duct; 3. Patients who are allergic to iodine or indocyanine green.

Design outcomes

Primary

MeasureTime frame
the incidence rate of postoperative chylothorax;—

Secondary

MeasureTime frame
surgery duration;volume of perioperative bleeding;volume of drainage;duration of chest tube;postoperative stay;incidence rate of postoperative pulmonary and cardiac complications;—

Countries

China

Contacts

Public ContactWenxin Tian

Beijing Hospital

georgetwx@163.com+86 138 1018 7942

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026